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Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events

A microneedle puncture of the fibroblast or sea urchin egg surface rapidly evokes a localized exocytotic reaction that may be required for the rapid resealing that follows this breach in plasma membrane integrity (Steinhardt, R.A,. G. Bi, and J.M. Alderton. 1994. Science (Wash. DC). 263:390–393). Ho...

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Detalles Bibliográficos
Autores principales: Terasaki, Mark, Miyake, Katsuya, McNeil, Paul L.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139822/
https://www.ncbi.nlm.nih.gov/pubmed/9314529
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author Terasaki, Mark
Miyake, Katsuya
McNeil, Paul L.
author_facet Terasaki, Mark
Miyake, Katsuya
McNeil, Paul L.
author_sort Terasaki, Mark
collection PubMed
description A microneedle puncture of the fibroblast or sea urchin egg surface rapidly evokes a localized exocytotic reaction that may be required for the rapid resealing that follows this breach in plasma membrane integrity (Steinhardt, R.A,. G. Bi, and J.M. Alderton. 1994. Science (Wash. DC). 263:390–393). How this exocytotic reaction facilitates the resealing process is unknown. We found that starfish oocytes and sea urchin eggs rapidly reseal much larger disruptions than those produced with a microneedle. When an ∼40 by 10 μm surface patch was torn off, entry of fluorescein stachyose (FS; 1,000 mol wt) or fluorescein dextran (FDx; 10,000 mol wt) from extracellular sea water (SW) was not detected by confocal microscopy. Moreover, only a brief (∼5–10 s) rise in cytosolic Ca(2+) was detected at the wound site. Several lines of evidence indicate that intracellular membranes are the primary source of the membrane recruited for this massive resealing event. When we injected FS-containing SW deep into the cells, a vesicle formed immediately, entrapping within its confines most of the FS. DiI staining and EM confirmed that the barrier delimiting injected SW was a membrane bilayer. The threshold for vesicle formation was ∼3 mM Ca(2+) (SW is ∼10 mM Ca(2+)). The capacity of intracellular membranes for sealing off SW was further demonstrated by extruding egg cytoplasm from a micropipet into SW. A boundary immediately formed around such cytoplasm, entrapping FDx or FS dissolved in it. This entrapment did not occur in Ca(2+)-free SW (CFSW). When egg cytoplasm stratified by centrifugation was exposed to SW, only the yolk platelet–rich domain formed a membrane, suggesting that the yolk platelet is a critical element in this response and that the ER is not required. We propose that plasma membrane disruption evokes Ca(2+) regulated vesicle–vesicle (including endocytic compartments but possibly excluding ER) fusion reactions. The function in resealing of this cytoplasmic fusion reaction is to form a replacement bilayer patch. This patch is added to the discontinuous surface bilayer by exocytotic fusion events.
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spelling pubmed-21398222008-05-01 Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events Terasaki, Mark Miyake, Katsuya McNeil, Paul L. J Cell Biol Article A microneedle puncture of the fibroblast or sea urchin egg surface rapidly evokes a localized exocytotic reaction that may be required for the rapid resealing that follows this breach in plasma membrane integrity (Steinhardt, R.A,. G. Bi, and J.M. Alderton. 1994. Science (Wash. DC). 263:390–393). How this exocytotic reaction facilitates the resealing process is unknown. We found that starfish oocytes and sea urchin eggs rapidly reseal much larger disruptions than those produced with a microneedle. When an ∼40 by 10 μm surface patch was torn off, entry of fluorescein stachyose (FS; 1,000 mol wt) or fluorescein dextran (FDx; 10,000 mol wt) from extracellular sea water (SW) was not detected by confocal microscopy. Moreover, only a brief (∼5–10 s) rise in cytosolic Ca(2+) was detected at the wound site. Several lines of evidence indicate that intracellular membranes are the primary source of the membrane recruited for this massive resealing event. When we injected FS-containing SW deep into the cells, a vesicle formed immediately, entrapping within its confines most of the FS. DiI staining and EM confirmed that the barrier delimiting injected SW was a membrane bilayer. The threshold for vesicle formation was ∼3 mM Ca(2+) (SW is ∼10 mM Ca(2+)). The capacity of intracellular membranes for sealing off SW was further demonstrated by extruding egg cytoplasm from a micropipet into SW. A boundary immediately formed around such cytoplasm, entrapping FDx or FS dissolved in it. This entrapment did not occur in Ca(2+)-free SW (CFSW). When egg cytoplasm stratified by centrifugation was exposed to SW, only the yolk platelet–rich domain formed a membrane, suggesting that the yolk platelet is a critical element in this response and that the ER is not required. We propose that plasma membrane disruption evokes Ca(2+) regulated vesicle–vesicle (including endocytic compartments but possibly excluding ER) fusion reactions. The function in resealing of this cytoplasmic fusion reaction is to form a replacement bilayer patch. This patch is added to the discontinuous surface bilayer by exocytotic fusion events. The Rockefeller University Press 1997-10-06 /pmc/articles/PMC2139822/ /pubmed/9314529 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Terasaki, Mark
Miyake, Katsuya
McNeil, Paul L.
Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events
title Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events
title_full Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events
title_fullStr Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events
title_full_unstemmed Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events
title_short Large Plasma Membrane Disruptions Are Rapidly Resealed by Ca(2+)-dependent Vesicle–Vesicle Fusion Events
title_sort large plasma membrane disruptions are rapidly resealed by ca(2+)-dependent vesicle–vesicle fusion events
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139822/
https://www.ncbi.nlm.nih.gov/pubmed/9314529
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